Production Method 1

555-16-8

79865-89-7

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: 2,5-Dihydroxyterephthalic acid (complexes with metals) ,  Magnesium ,  Nickel ,  Cobalt (complexes with 2,5-Dihydroxyterephthalic acid) ;  7 h, 160 °C

Reference

Boosting performance for hydrogenation-alkylation tandem reaction catalyzed by banana-like MgO-based solid solution confined Ni-Co alloy catalyst: Fabricated by a MTV-MOFs templated strategy

Li, Weizuo; et al, Molecular Catalysis, 2022, 529,

Production Method 2

459-57-4

79865-89-7

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Dimethyl sulfoxide ;  3 d, 95 °C
1.2 Solvents: Water

Reference

Design, synthesis, and evaluation of resveratrol derivatives as Ass1-42 aggregation inhibitors, antioxidants, and neuroprotective agents

Lu, Chuanjun; et al, Bioorganic & Medicinal Chemistry Letters, 2012, 22(24), 7683-7687

Production Method 3

79865-85-3

79865-89-7

Reaction Conditions

Reference

Substitution of the methoxy group in p-[methoxybenzylidene]dimethylimmonium iodide

Yudin, L. G.; et al, Zhurnal Organicheskoi Khimii, 1981, 17(8), 1785-6

Production Method 4

79865-88-6

79865-89-7

Reaction Conditions

Reference

Substitution of the methoxy group in p-[methoxybenzylidene]dimethylimmonium iodide

Yudin, L. G.; et al, Zhurnal Organicheskoi Khimii, 1981, 17(8), 1785-6

Production Method 5

13114-23-3

79865-89-7

Reaction Conditions

Reference

Activating action of an immonium group in replacement of alkoxyl and halo atom by alkylamino group in the benzene ring

Yudin, L. G.; et al, Zhurnal Organicheskoi Khimii, 1983, 19(11), 2361-6

Production Method 6

555-16-8

79865-89-7

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Cobalt dinitrate (poly. with hexamethylenetetramine) ;  13 h, 2 MPa, 170 °C

Reference

A strategy of two-step tandem catalysis towards direct N-alkylation of nitroarenes with ethanol via facile fabricated novel Co-based catalysts derived from coordination polymers

Wang, Jing; et al, Journal of Catalysis, 2019, 376, 106-118

Production Method 7

459-57-4

79865-89-7

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Tetrabutylammonium bromide Solvents: Dimethyl sulfoxide ;  48 h, rt → 90 °C

Reference

The Role of N-Substituents in Radiationless Deactivation of Aminated Derivatives of a Locked GFP Chromophore

Baleeva, Nadezhda S.; et al, European Journal of Organic Chemistry, 2017, 2017(35), 5219-5224

Production Method 8

459-57-4

79865-89-7

Reaction Conditions

1.1 Solvents: Water ;  15 h, 130 °C

Reference

A BODIPY fluorescence probe modulated by selenoxide spirocyclization reaction for peroxynitrite detection and imaging in living cells

Wang, Bingshuai; et al, Dyes and Pigments, 2013, 96(2), 383-390

Production Method 9

79865-85-3

79865-89-7

Reaction Conditions

Reference

Activating action of an immonium group in replacement of alkoxyl and halo atom by alkylamino group in the benzene ring

Yudin, L. G.; et al, Zhurnal Organicheskoi Khimii, 1983, 19(11), 2361-6

Production Method 10

123-11-5

79865-89-7

Reaction Conditions

Reference

Replacement of the alkylamino group in p-substituted benzaldehydes

Yudin, L. G.; et al, Zhurnal Organicheskoi Khimii, 1982, 18(2),

Production Method 11

123-11-5

79865-89-7

Reaction Conditions

Reference

Activating action of an immonium group in replacement of alkoxyl and halo atom by alkylamino group in the benzene ring

Yudin, L. G.; et al, Zhurnal Organicheskoi Khimii, 1983, 19(11), 2361-6

Production Method 12

555-16-8

79865-89-7

120-21-8

Reaction Conditions

1.1 Reagents: Water Catalysts: Platinum, compd. with tin (3:1) ;  5 MPa, 503 K

Reference

Heterogeneously catalyzed one-pot synthesis of N-alkyl anilines from nitroaromatics by assembled Pt3Sn/Al2O3 catalyst

Yang, Fang; et al, Wuli Huaxue Xuebao, 2012, 28(9), 2141-2147

4-(Ethylamino)benzaldehyde Raw materials

• 4-Nitrobenzaldehyde
• 4-Fluorobenzaldehyde
• Methanaminium, N-[[4-(ethylamino)phenyl]methylene]-N-methyl-, iodide
• p-Methoxybenzaldehyde
• Methanaminium, N-[(4-methoxyphenyl)methylene]-N-methyl-, iodide
• N-(4-Methoxybenzylidene)methanamine

4-(Ethylamino)benzaldehyde Preparation Products

• 4-Diethylaminobenzaldehyde (120-21-8)
• 4-(Ethylamino)benzaldehyde (79865-89-7)

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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoyl derivatives

• 120-21-8(4-Diethylaminobenzaldehyde)
• 84281-72-1(benzaldehyde, reaction products with n,n-diethylbenzenamine and n,n-dimethylbenzenamine, oxidized)
• 613-28-5(4-(Dipropylamino)benzaldehyde)
• 339062-76-9(3-(Methylamino)benzaldehyde)
• 84238-44-8(Benzaldehyde, reaction products with N,N-diethylbenzenamine and N,N-dimethylbenzenamine, oxidized, chlorides)
• 89074-18-0(Benzaldehyde, 4-(butylamino)-)
• 86872-96-0(4-ethyl(phenyl)aminobenzaldehyde)
• 78575-81-2(Benzaldehyde, 4,4'-[1,3-propanediylbis(methylimino)]bis-)
• 556-21-8(4-(Methylamino) benzaldehyde)
• 784102-54-1(Benzaldehyde, 3-(1-aziridinyl)- (9CI))